This study aimed to evaluate the in vivo anticancer effects of
daucosterol which was earlier reported to possess in vitro anticancer effects.
Breast tumor was induced in 30 rats using the environmental
carcinogen 7,12-dimethylbenz(a)anthracene (DMBA) while 6 control rats received
olive oil (NOR). Animals with palpable
tumors were randomized into five groups (n = 6) each as follows: negative control group treated with the vehicle (DMBA); positive control group treated with 5 mg/kg BW
doxorubicin (DOXO + DMBA); three groups treated with
daucosterol at doses of 2.5, 5, and 10 mg/kg BW (DAU + DMBA). Treatment lasted 28 days afterward,
tumor (mass, volume,
cancer antigen [CA] 15-3 level and histoarchitecture), hematological and toxicological parameters were examined. The
tumor volume gradually increased in the DMBA group during the 28 days, with a
tumor volume gain of ∼390 cm3 .
Daucosterol at all doses reduced
tumor volume (∼133.7 cm3 at 10 mg/kg) as well as
protein,
malondialdehyde (MDA), and CA 15-3 levels compared to DMBA rats.
Tumor sections in
daucosterol-treated rats showed a lower proliferation of mammary ducts with mild (5 and 10 mg/kg) to moderate (2.5 mg/kg) inflammatory responses. Moreover, it exhibited an
antioxidant effect, evidenced by a significant and dose-dependent decreased in MDA levels, as well as an increase in
catalase activity compared to the DMBA group.
Daucosterol showed for the first time in vivo antitumor effects that corroborate its previous in vitro effects.